A convenient reduction of N-(2-substituted-1-cyanoethenyl) acetamides with NaTeH

Article abstract of DOI:10.1080/00397919708004213

N-(1-cyano-2-substituted phenylethyl) acetamides (4a-h) were synthesized by reduction of corresponding titled compounds 3a-h with NaTeH. The procedure was general and convenient for preparation of benzyl substituted acyclic Reissert compounds without usin

Full text of DOI:10.1080/00397919708004213

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A Convenient Reduction
Of N-(2-Substituted-1-
cyanoethenyl) Acetamides
with NaTeH
Pengju Zeng a , Yuefei Hu a b & Hongwen Hu a
a Department of Chemistry , Nanjing University ,
Nanjing, 210093, People's Republic of China
b Coordination Chemistry Institute, Nanjing
University , Nanjing, 210093, People's Republic
of China
Published online: 22 Aug 2006.
To cite this article: Pengju Zeng , Yuefei Hu & Hongwen Hu (1997) A Convenient
Reduction Of N-(2-Substituted-1-cyanoethenyl) Acetamides with NaTeH, Synthetic
Communications: An International Journal for Rapid Communication of Synthetic
Organic Chemistry, 27:5, 939-944, DOI: 10.1080/00397919708004213
To link to this article: http://dx.doi.org/10.1080/00397919708004213
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